Label: TIGER BALM PAIN RELIEVING HYDROGEL LARGE (camphor- synthetic, levomenthol, and capsicum patch
- NDC Code(s): 66761-324-04
- Packager: Haw Par Healthcare Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 5, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
-
Warnings
FOR EXTERNAL USE ONLY
When using this product
- Use only as directed
- Do not get into eyes or on mucous membranes
- Do not apply to wounds, damaged or irritated skin
- Do not bandage or cover with any type of wrap except clothing
- Do not use with a heating pad or apply external heat
- Do not use 1 hour prior to bathing or within 30 minutes after bathing
Stop use and ask a doctor if
- Condition worsens
- Severe skin irritation occurs
- Pain persists for more than 7 days
- Symptoms clear up and occur again within a few days
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Directions
- Adults and children 12 years and over apply to affected area; change patch 1 to 2 times daily
- Children under 12 years, consult doctor before use
- How to apply:
- Clean and dry affected area
- Cut open pouch and remove patch
- Remove protective film and apply directly to area of pain
- Apply to affected area not more than 3 times daily
- Wash hands with soap after applying patch
- Reseal pouch containing unused patches
- Other Information
- Inactive Ingredients
- Questions/Comments
- PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Label
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INGREDIENTS AND APPEARANCE
TIGER BALM PAIN RELIEVING HYDROGEL LARGE
camphor (synthetic), levomenthol, and capsicum patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66761-324 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 230 mg LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL 70 mg CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM 46 mg Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) eucalyptus oil (UNII: 2R04ONI662) glycerin (UNII: PDC6A3C0OX) methyl acrylate (UNII: WC487PR91H) water (UNII: 059QF0KO0R) polysorbate 80 (UNII: 6OZP39ZG8H) silicon dioxide (UNII: ETJ7Z6XBU4) sorbitan monooleate (UNII: 06XEA2VD56) sorbitol (UNII: 506T60A25R) tartaric acid (UNII: W4888I119H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66761-324-04 1 in 1 BOX 01/01/2017 1 4 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M017 01/01/2017 Labeler - Haw Par Healthcare Ltd. (659207039)